Development of left ventricular hypertrophy in adults with hypertrophic cardiomyopathy caused by cardiac myosin-binding protein C gene mutations
Open Access
- 18 August 2001
- journal article
- Published by Elsevier in Journal of the American College of Cardiology
- Vol. 38 (2) , 315-321
- https://doi.org/10.1016/s0735-1097(01)01386-9
Abstract
No abstract availableKeywords
This publication has 28 references indexed in Scilit:
- Magnitude of Left Ventricular Hypertrophy and Risk of Sudden Death in Hypertrophic CardiomyopathyNew England Journal of Medicine, 2000
- Cardiac myosin binding protein–C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathyNature Genetics, 1995
- Mutations in the cardiac myosin binding protein–C gene on chromosome 11 cause familial hypertrophic cardiomyopathyNature Genetics, 1995
- The standard electrocardiogram as a screening test for hypertrophic cardiomyopathyThe American Journal of Cardiology, 1995
- Relation of electrocardiographic abnormalities to evolving left ventricular hypertrophy in hypertrophic cardiomyopathy during childhoodThe American Journal of Cardiology, 1989
- Development and Progression of Left Ventricular Hypertrophy in Children with Hypertrophic CardiomyopathyNew England Journal of Medicine, 1986
- Hypertrophic cardiomyopathy. The importance of the site and the extent of hypertrophy. A reviewProgress in Cardiovascular Diseases, 1985
- Systolic anterior motion of the posterior mitral leaflet: a previously unrecognized cause of dynamic subaortic obstruction in patients with hypertrophic cardiomyopathy.Circulation, 1983
- Hypertrophie cardiomyopathy: A discussion of nomenclatureThe American Journal of Cardiology, 1979
- Recommendations regarding quantitation in M-mode echocardiography: results of a survey of echocardiographic measurements.Circulation, 1978